The University of Arizona, Tucson, AZ, USA; Arizona Alzheimer's Consortium, Phoenix, AZ, USA.
Translational Genomics Research Institute, Phoenix, AZ, USA; Arizona Alzheimer's Consortium, Phoenix, AZ, USA.
Trends Neurosci. 2023 Sep;46(9):750-763. doi: 10.1016/j.tins.2023.06.003. Epub 2023 Jul 16.
The apolipoprotein ε4 (APOE ε4) allele is most commonly associated with increased risk for late-onset Alzheimer's disease (AD). However, recent longitudinal studies suggest that these risks are overestimated; most ε4 carriers will not develop dementia in their lifetime. In this article, we review new evidence regarding the impact of APOE ε4 on cognition among healthy older adults. We discuss emerging work from animal models suggesting that ε4 impacts brain structure and function in multiple ways that may lead to age-related cognitive impairment, independent from AD pathology. We discuss the importance of taking an individualized approach in future studies by incorporating biomarkers and neuroimaging methods that may better disentangle the phenotypic influences of APOE ε4 on the aging brain from prodromal AD pathology.
载脂蛋白 E4(APOE ε4)等位基因与晚发性阿尔茨海默病(AD)的风险增加最为相关。然而,最近的纵向研究表明,这些风险被高估了;大多数 ε4 携带者在其一生中不会发展为痴呆。在本文中,我们回顾了关于 APOE ε4 对健康老年人认知的影响的新证据。我们讨论了来自动物模型的新工作,这些工作表明 ε4 以多种方式影响大脑结构和功能,这可能导致与 AD 病理学无关的与年龄相关的认知障碍。我们讨论了在未来的研究中采用个体化方法的重要性,该方法纳入生物标志物和神经影像学方法,可能会更好地从 AD 病理的前驱期将 APOE ε4 对衰老大脑的表型影响分离开来。